Premium
Rearrangement and Fragmentation of Pentaphenylazetidinone
Author(s) -
Sarel S.,
Breuer E.,
Klug J. T.,
Fattal Y.
Publication year - 1966
Publication title -
israel journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.908
H-Index - 54
eISSN - 1869-5868
pISSN - 0021-2148
DOI - 10.1002/ijch.196600037
Subject(s) - chemistry , fragmentation (computing) , benzophenone , aluminum hydride , sulfuric acid , hydride , photochemistry , medicinal chemistry , inorganic chemistry , organic chemistry , ion , hydrogen , computer science , operating system , methoxide
1, 3, 3, 4, 4‐Pentaphenylazetidinone‐2 (I) is converted by sulfuric acid into 1, 3, 3, 4‐tetraphenylhydrocarbostyril. Upon treatment with lithium aluminum hydride (I) undergoes a fragmentation reaction from which benzophenone anil is isolated.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom